Institute for Computational Systems Biology, University of Hamburg, Hamburg 22607, Germany.
Department of Medicine, Hamburg Center for Translational Immunology (HCTI) and Center for Biomedical AI (bAIome), University Medical Center Hamburg-Eppendorf (UKE), Hamburg 20246, Germany.
Bioinformatics. 2023 Nov 1;39(11). doi: 10.1093/bioinformatics/btad644.
The reconstruction of small key regulatory networks that explain the differences in the development of cell (sub)types from single-cell RNA sequencing is a yet unresolved computational problem.
To this end, we have developed SCANet, an all-in-one package for single-cell profiling that covers the whole differential mechanotyping workflow, from inference of trait/cell-type-specific gene co-expression modules, driver gene detection, and transcriptional gene regulatory network reconstruction to mechanistic drug repurposing candidate prediction. To illustrate the power of SCANet, we examined data from two studies. First, we identify the drivers of the mechanotype of a cytokine storm associated with increased mortality in patients with acute respiratory illness. Secondly, we find 20 drugs for eight potential pharmacological targets in cellular driver mechanisms in the intestinal stem cells of obese mice.
SCANet is a free, open-source, and user-friendly Python package that can be seamlessly integrated into single-cell-based systems medicine research and mechanistic drug discovery.
从单细胞 RNA 测序重建解释细胞(亚)类型发育差异的小型关键调控网络是一个尚未解决的计算问题。
为此,我们开发了 SCANet,这是一个用于单细胞分析的一体化软件包,涵盖了整个差异机械分型工作流程,从推断特征/细胞类型特异性基因共表达模块、驱动基因检测以及转录基因调控网络重建到机制药物再利用候选物预测。为了说明 SCANet 的强大功能,我们检查了来自两项研究的数据。首先,我们确定了与急性呼吸道疾病患者死亡率升高相关的细胞因子风暴机械型的驱动因素。其次,我们在肥胖小鼠肠道干细胞中发现了 20 种针对八种潜在药理靶点的药物。
SCANet 是一个免费的、开源的、用户友好的 Python 软件包,可以无缝集成到基于单细胞的系统医学研究和机制药物发现中。